2004•Bulletin of Science and TechnologyRequires access

Effects of IGF-II on MC3T3-E1 Cells Proliferation and Nitric Oxide Production

Sun Wei-lian

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Abstract

ObjectiveTo study the effects of IGF-II on cell proliferation and nitric oxide content in MC3T3-E1 osteoblast.MethodsMouse calvaria-derived osteoblastic clone MC3T3-E1 cell line were incubated with different concentrations of IGF-II in α-MEM culture medium. Cell proliferation was determined by MTT and the nitric oxide concentration in the culture medium was measured by enzyme assay. ResultsOver a concentration range of 1~100 ng/mL, IGF-II promoted MC3T3-E1 cells proliferation in a dose-dependent manner, and it also significantly decreased the level of nitric oxide in the 100 ng/mL group at the third day (P0.01); the OD value of the control group at the sixth day was evidently lower than that of at the fifth day (P(0.01)),while the OD value of the 100 ng/mL group at the sixth day was obviously higher than that of at the fifth day (P0.01). ConclusionIGF-II can promote cell proliferation, inhibit NO production, and can significantly prevent cell death of MC3T3-E1.

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ObjectiveTo study the effects of IGF-II on cell proliferation and nitric oxide content in MC3T3-E1 osteoblast.MethodsMouse calvaria-derived osteoblastic clone MC3T3-E1 cell line were incubated with different concentrations of IGF-II in α-MEM culture medium. Cell proliferation was determined by MTT and the nitric oxide concentration in the culture medium was measured by enzyme assay. ResultsOver a concentration range of 1~100 ng/mL, IGF-II promoted MC3T3-E1 cells proliferation in a dose-dependent manner, and it also significantly decreased the level of nitric oxide in the 100 ng/mL group at the third day (P0.01); the OD value of the control group at the sixth day was evidently lower than that of at the fifth day (P(0.01)),while the OD value of the 100 ng/mL group at the sixth day was obviously higher than that of at the fifth day (P0.01). ConclusionIGF-II can promote cell proliferation, inhibit NO production, and can significantly prevent cell death of MC3T3-E1.

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Available abstract

ObjectiveTo study the effects of IGF-II on cell proliferation and nitric oxide content in MC3T3-E1 osteoblast.MethodsMouse calvaria-derived osteoblastic clone MC3T3-E1 cell line were incubated with different concentrations of IGF-II in α-MEM culture medium. Cell proliferation was determined by MTT and the nitric oxide concentration in the culture medium was measured by enzyme assay. ResultsOver a concentration range of 1~100 ng/mL, IGF-II promoted MC3T3-E1 cells proliferation in a dose-dependent manner, and it also significantly decreased the level of nitric oxide in the 100 ng/mL group at the third day (P0.01); the OD value of the control group at the sixth day was evidently lower than that of at the fifth day (P(0.01)),while the OD value of the 100 ng/mL group at the sixth day was obviously higher than that of at the fifth day (P0.01). ConclusionIGF-II can promote cell proliferation, inhibit NO production, and can significantly prevent cell death of MC3T3-E1.

Key concepts: Nitric oxide, Calvaria, Cell growth, Cell culture, Chemistry, Cell division, clone (Java method), Andrology

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